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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 13263생성일: 2026년 10월 26일

브로목시닐

브로목시닐 · Bromoxynil · AMETRYNE · AMETREX · Ametrine · Ametrin · EVIK · a1093

https://huagongshe.com/ko/chemical/13263

브로목시닐 분자 구조식

식별자 및 물리적 특성

CAS No.834-12-8
분자식C9H17N5S
평균 분자량227.33 g/mol
단동위원소 질량227.12046674 g/mol
SMILESCCNc1nc(NC(C)C)nc(SC)n1
InChIKeyRQVYBGPQFYCBGX-UHFFFAOYSA-N
PubChem CID13263
ChEMBLCHEMBL1235774
ChEBICHEBI:22472
EC No.212-634-7
DTXSIDDTXSID1023869
현지명브로목시닐

화학 및 물리적 성질

XLogP3
극성 표면적88
수소 결합 공여자 수2
수소 결합 수용자 수6
회전 가능 결합 수5
무거운 원자 수15
형식 전하0
복잡도178
녹는점84-85°C
끓는 점310.44°C (rough estimate)
밀도1.1232 (rough estimate)
증기압0Pa at 20℃
굴절률1.5500 (estimate)
인화점11 °C
저장 조건Keep in dark place,Sealed in dry,2-8°C
용해도클로로포름(약간 용해됨), DMSO(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태수정 같은
pKa(산도 계수)3.71±0.41(Predicted)
색상White to off-white
용해도209mg/L(25℃)
Merck13,391
BRN613099
헨리 상수2.1×101 mol/(m3Pa) at 25℃, Chao et al. (2017)
주요 응용농업환경
InChI1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)
InChIKeyRQVYBGPQFYCBGX-UHFFFAOYSA-N
SMILESCCNc1nc(NC(C)C)nc(SC)n1
LogP(분배 계수)3 at 20℃
NIST1,3,5-Triazine-2,4-diamine, N-ethyl-N'-(1-methylethyl)-6-(methylthio)-(834-12-8)
EPAAmetryn (834-12-8)

화학적 성질

Ametryn is a colorless powder

안전 및 규제

수질 위해 등급(WGK)3
RTECS 번호XY9100000
운송 번호(UN)UN 1230 3/PG 2
독성LD50 in adult male, female rats (mg/kg): 508, 590 orally (Gaines, Linder)
관세 코드29336990
위험 문구(R)22-50/53-39/23/24/25-23/24/25-11
위험 표시XnN,N,Xn,T,F
안전 문구(S)2-36-60-61-45-16-7
위험 등급Acute Tox. 4 OralAquatic Acute 1Aquatic Chronic 1
저장 분류13 - Non Combustible Solids
유해 물질 데이터834-12-8(Hazardous Substances Data)

용도

용도

Ametryn is a methylthiotriazine based herbicide which inhibits photosynthesis and other enzymatic processes. Ametryn is used to control broadleaf weeds and annual grasses in pineapple, sugarcane and b ananas.

일반 설명

Crystals. Melting point 190-192°F (88-89°C). Used as a herbicide.

제조 및 합성 방법

생산 방법

Ametryn is a colorless crystal synthesized by reacting atrazine with methyl mercaptan in the presence of an equivalent of NaOH or by reacting 2-mercapto-4-ethylamino-6-isopropylamino- 1,3,5-triazine with a methylating agent in the presence of NaOH. It is stable in slightly acidic or alkaline media, but is hydrolyzed to the inactive 6-hydroxy derivative in strong acidic or basic media.